Evidence map›Paper›PMID 33282178›Full record

ArticlePulmonary circulation

Autologous correction in patient induced pluripotent stem cell-endothelial cells to identify a novel pathogenic mutation of hereditary hemorrhagic telangiectasia.

Fang Zhou, Xiuli Zhao, Xiu Liu, Yanyan Liu, Feng Ma, Bao Liu, Jun Yang

Open access · goldAbstract read
In one paragraph

Article in Pulmonary circulation. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.1field-weighted citation impact, top 45% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Fang ZhouDepartment of Cell Biology, Chinese Academy of Medical Sciences and School of Basic Medicine, Beijing, China.ORCID https://orcid.org/0000-0002-3066-185X
Xiuli ZhaoDepartment of Genetics, Chinese Academy of Medical Sciences and School of Basic Medicine, Beijing, China.
Xiu LiuDepartment of Vascular Surgery, Chinese Academy of Medical Science and Peking Union Medical College, Beijing, China.
Yanyan LiuDepartment of Cell Biology, Chinese Academy of Medical Sciences and School of Basic Medicine, Beijing, China.
Feng MaState Key Laboratory of Experimental Hematology, Institute of Hematology & Blood Diseases Hospital, Tianjin, China.
Bao LiuDepartment of Vascular Surgery, Chinese Academy of Medical Science and Peking Union Medical College, Beijing, China.
Jun YangDepartment of Cell Biology, Chinese Academy of Medical Sciences and School of Basic Medicine, Beijing, China.ORCID https://orcid.org/0000-0001-9715-8100
Chinese Academy of Medical Sciences & Peking Union Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hereditary hemorrhagic telangiectasia is a rare disease with autosomal dominant inheritance. More than 80% hereditary hemorrhagic telangiectasia patients carry heterozygous mutations of

Indexed as

Endoglinhereditary hemorrhagic telangiectasia (HHT)induced pluripotent stem cell (iPSC) differentiated endothelial cells

Identifiers

PMID33282178
PMCPMC7691931
OpenAlexW2979375433

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.